| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:25287243-25287572 | Common:2; Rare:102 | ||||
| chr13:25301485-25301759 | Common:2; Rare:101 | ||||
| chr13:26221787-26221982 | Rare:57 | ||||
| chr13:27251235-27251616 | Common:7; Rare:117 | ||||
| chr13:27253675-27253867 | Common:1; Rare:44 | ||||
| chr13:27424521-27424732 | Common:2; Rare:68 | ||||
| chr13:27450124-27450230 | Common:3; Rare:31 | ||||
| chr13:27450519-27450657 | Common:2; Rare:57 | ||||
| chr13:27620480-27620812 | Common:2; Rare:109 | ||||
| chr13:28138133-28138234 | Common:1; Rare:31 | ||||
| chr13:28659076-28659187 | Rare:49; Clinvar (pathogenic):1 | ||||
| chr13:28718771-28719126 | Common:1; Rare:92 | ||||
| chr13:30306840-30307223 | Common:6; Rare:107 | ||||
| chr13:30307368-30307606 | Common:3; Rare:78 | ||||
| chr13:30464868-30465025 | Common:1; Rare:44 |